Canonical Allele Identifier: CA344521472

Gene: CD55

Linked Data

• dbSNP Id: rs1655217495
• gnomAD v4: 1-207337191-T-A
• MyVariant Identifiers: chr1:g.207510536T>A (hg19) ; chr1:g.207337191T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207337191T>A , CM000663.2:g.207337191T>A	GRCh38
NC_000001.10:g.207510536T>A , CM000663.1:g.207510536T>A	GRCh37
NC_000001.9:g.205577159T>A	NCBI36
NG_007465.1:g.20720T>A , LRG_127:g.20720T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695822.1:n.1227-138T>A
ENST00000695823.1:c.791-138T>A	ENSP00000512200.1:n.791-138T>A
ENST00000695824.1:c.980-138T>A	ENSP00000512201.1:n.980-138T>A
ENST00000695825.1:c.980-138T>A	ENSP00000512202.1:n.980-138T>A
ENST00000695826.1:c.980-138T>A	ENSP00000512203.1:n.980-138T>A
ENST00000695827.1:n.1580T>A
ENST00000695828.1:c.791-138T>A	ENSP00000512204.1:n.791-138T>A
ENST00000695831.1:n.614T>A
ENST00000367064.9:c.980-138T>A MANE Select	ENSP00000356031.4:n.980-138T>A
ENST00000391921.9:c.788-138T>A	ENSP00000375788.4:n.788-138T>A
ENST00000488171.6:n.595-138T>A
ENST00000618707.2:c.484-138T>A
ENST00000635614.2:c.322-138T>A
ENST00000644836.1:c.980-138T>A	ENSP00000495518.1:n.980-138T>A
ENST00000645323.1:c.980-138T>A	ENSP00000496251.1:n.980-138T>A
ENST00000314754.12:c.980-138T>A	ENSP00000316333.8:n.980-138T>A
ENST00000367063.6:c.980-138T>A	ENSP00000356030.2:n.980-138T>A
ENST00000367064.7:c.980-138T>A	ENSP00000356031.3:n.980-138T>A
ENST00000367067.8:c.1349T>A	ENSP00000356034.5:p.Leu450Gln
ENST00000391921.8:c.788-138T>A	ENSP00000375788.4:n.788-138T>A
ENST00000465534.5:n.967T>A
ENST00000476590.1:n.967T>A
ENST00000488171.5:n.1059-138T>A
ENST00000634386.1:n.66-138T>A
ENST00000635614.1:n.316-138T>A
NM_000574.4:c.980-138T>A	NP_000565.1:n.980-138T>A
NM_001114752.2:c.980-138T>A	NP_001108224.1:n.980-138T>A
NM_001300902.1:c.980-138T>A	NP_001287831.1:n.980-138T>A
NM_001300903.1:c.980-138T>A	NP_001287832.1:n.980-138T>A
NM_001300904.1:c.980-138T>A	NP_001287833.1:n.980-138T>A
NR_125349.1:n.1274-138T>A
XM_017000467.2:c.980-138T>A	XP_016855956.1:n.980-138T>A
NM_000574.5:c.980-138T>A MANE Select	NP_000565.1:n.980-138T>A
NM_001114752.3:c.980-138T>A	NP_001108224.1:n.980-138T>A
NM_001300902.2:c.980-138T>A	NP_001287831.1:n.980-138T>A
NM_001300903.2:c.980-138T>A	NP_001287832.1:n.980-138T>A
NM_001300904.2:c.980-138T>A	NP_001287833.1:n.980-138T>A
NR_125349.2:n.1068-138T>A